ライフサイエンスコーパス: phyllosphere

1 to the above ground portions of plants (the phyllosphere).

2 an influential role in structuring the leaf phyllosphere.

3 o be absorbed in complex exchange within the phyllosphere.

4 ves changes in bacterial colonization of the phyllosphere.

5 er richness and diversity of bacteria at the phyllosphere.

6 unities of the tomato (Solanum lycopersicum) phyllosphere.

7 important step in bacterial infection of the phyllosphere.

8 ophytic commensal bacterial community in the phyllosphere.

9 ntibiotics or competing for nutrients in the phyllosphere.

10 isease epidemiology, and microbiology of the phyllosphere.

11 h the exception of the rspC promoter) in the phyllosphere.

12 dual E. herbicola cells as they colonize the phyllosphere.

13 these sugars to microbial colonizers of the phyllosphere.

14 by its requirement for growth of Pss in the phyllosphere.

15 an insects are ubiquitous inhabitants of the phyllosphere.

16 udomonas strains in the Arabidopsis thaliana phyllosphere.

17 microbial communities in the rhizosphere and phyllosphere.

18 imary biomarkers for both bulk soils and the phyllosphere.

19 lism in the individual microbial taxa in the phyllosphere affected by irrigation and mycorrhizal asso

20 nomic diversity of P. syringae in the cherry phyllosphere and focused on the role of prophages in tra

21 oles in promoting microbial diversity in the phyllosphere and highlights the importance of plant-micr

22 l importance of bacterial communities in the phyllosphere and rhizosphere of plants, a more detailed

23 ents, including the mammalian gut, the plant phyllosphere and rhizosphere, soil, freshwaters and ocea

24 yo and pericarp and the developing seeding's phyllosphere and root systems were analysed using amplic

25 at priority effects and interactions between phyllosphere and soil organisms can help explain the pos

26 Here, we characterized the phyllosphere and soil protistan communities associated w

27 s define the vulnerability of species in the phyllosphere, and beyond, to thermal extremes.

28 and composition of protists in sorghum leaf phyllosphere, and rhizosphere and bulk soils, collected

29 rhizosphere was the opposite to that in the phyllosphere, and the higher number and activity of E. c

30 cantly higher diversity of protists than the phyllosphere, and the protistan community structure sign

31 anisms in above-ground habitats, such as the phyllosphere, and their potential role in CO cycling rem

32 ributes that drive community assembly in the phyllosphere are poorly understood.

33 However, the dynamic changes of phyllosphere-associated microbiome during pathogen infec

34 can help explain the positive effects of the phyllosphere at home, and suggest a path forward for fur

35 d Burkholderiales which were abundant in the phyllosphere at the time of sampling.

36 study, we comprehensively characterized tree phyllosphere bacteria and associated nutrient-cycling ge

37 We estimated that at least 25% of the phyllosphere bacteria collected from the plants grown in

38 bunits demonstrated that, on average, 25% of phyllosphere bacteria contained CO-dehydrogenase gene ho

39 phere community members, an estimated 21% of phyllosphere bacteria contained CoxL, the large subunit

40 Phyllosphere bacteria were identified from Citrus sinesi

41 es had 97--100% similarity to those of known phyllosphere bacteria, but only two of them matched thos

42 trains that had been described previously as phyllosphere bacteria.

43 Phyllosphere bacterial communities have the potential to

44 processes primarily governed the assembly of phyllosphere bacterial communities, although the role of

45 onmental filters deterministically constrain phyllosphere bacterial communities.

46 hment of salt stress- and leaf age-dependent phyllosphere bacterial communities.

47 Results revealed that phyllosphere bacterial community diversity, richness, st

48 These correlations between phyllosphere bacterial diversity and host growth, mortal

49 nceptual framework for understanding diverse phyllosphere-bacterial interactions.

50 ng aqueous chemistry; (ii) the importance of phyllosphere biofilms in shaping leaf surface chemistry

51 tant role in enabling Pss to flourish in the phyllosphere, but not the spermosphere.

52 on their surfaces and in the rhizosphere and phyllosphere by a multitude of different microorganisms

53 gi in nutrient-limited environments like the phyllosphere by the novel mechanism of HI induction.

54 New insights into how the phyllosphere carries out key biological processes, inclu

55 ral pieces to this puzzle, utilizing a model phyllosphere colonizer Methylobacterium extorquens PA1.

56 urrence of HFA in the presence vs absence of phyllosphere communities and found that HFA effects were

57 Changes in microbial phyllosphere communities have recently been demonstrated

58 Like other studied ecosystems, microbial phyllosphere communities therefore are more complex than

59 and found that HFA effects were smaller when phyllosphere communities were removed.

60 ion routes for the establishment of root and phyllosphere communities.

61 relative proportion of soilborne bacteria in phyllosphere communities.

62 ity and strongly shifted the rhizosphere and phyllosphere community composition.

63 Based on predicted genomes of phyllosphere community members, an estimated 21% of phyl

64 on the foliage before litter fall (i.e. the phyllosphere community) may help us to better understand

65 Here, we investigated the phyllosphere composition of two common Nigerian medicina

66 ing glories (Ipomoea hederifolia L.) with 32 phyllosphere consortia of either low or high diversity o

67 ne dehalogenase cmuA gene in the A. thaliana phyllosphere correlated with HOL1 genotype, as shown by

68 If metabolic activity in the phyllosphere corresponds to a more prepared state of inf

69 sting that soil is an important reservoir of phyllosphere diversity.

70 us extra-leaf processes to the generation of phyllosphere dynamics is important to determining the ra

71 e about how individual microbes adapt to the phyllosphere environment and their role in providing bio

72 ated with aboveground tissues, termed 'plant-phyllosphere feedback (PPFs)'.

73 , we tested the combined effects of soil and phyllosphere feedback under field conditions.

74 of rulAB for survival of P. syringae in its phyllosphere habitat, coupled with its wide distribution

75 The phyllosphere has been estimated to make up around 60% of

76 terrestrial plants, collectively called the phyllosphere, have a key role in the global balance of a

77 determine the contributions of microbiota to phyllosphere health and productivity.

78 operly assembled leaf bacterial community in phyllosphere health.

79 nsive strategy against phytopathogens in the phyllosphere, highlighting the potential of symbiotic mi

80 between a specific plant metabolite and rice phyllosphere homeostasis opening possibilities for new b

81 However, phyllosphere (i.e., leaf) population sizes of the hrcC a

82 from a variety of environments including the phyllosphere, i.e. the aerial parts of vegetation.

83 ngal microbiome diversity, especially in the phyllosphere, impacts intermicrobial interactions and co

84 ecting the above-ground parts of plants (the phyllosphere) in crop fields and natural ecosystems, but

85 The microbial community residing on the phyllosphere is influenced by many factors, including th

86 aturally observed microbial community in the phyllosphere is likely transient or poorly adapted withi

87 Extension of the PSF framework to the phyllosphere is needed to more fully elucidate plant-mic

88 Overall, the phyllosphere is proving to be both an important microbia

89 As an open system, the phyllosphere is subjected to environmental perturbations

90 ial habitat influenced by plants, termed the phyllosphere, is particularly amenable to studies of mic

91 and resultantly increasing the abundance of phyllosphere lactic acid bacteria.

92 c and fungal communities in the rhizosphere, phyllosphere, leaf and root endosphere, as well as proxi

93 ss, mold, bark, and arboreal soil (hereafter phyllosphere), may store 10-100 times the contemporary f

94 t of this, data mining of publicly available phyllosphere metagenomes for genes encoding CO-dehydroge

95 e blast disease, needs to compete with other phyllosphere microbes and overcome host immunity for suc

96 Here, we found phyllosphere microbes can mitigate wheat Fusarium head b

97 Through sequencing 16S rRNA amplicons of phyllosphere microbes in the pl mutant, we show that ant

98 Decades of pioneering work using individual phyllosphere microbes, including commensals and pathogen

99 Phyllosphere microbial communities are a useful model sy

100 the first time the contribution of light and phyllosphere microbial communities of Quercus ilex leave

101 Phyllosphere microbial communities were evaluated on lea

102 confirming the degradation ability of native phyllosphere microbial communities.

103 changed the structure and composition of the phyllosphere microbial community.

104 Fruit decomposition decreased phyllosphere microbial diversity and strongly shifted th

105 n and neighbourhood conditions in supporting phyllosphere microbial diversity remains poorly understo

106 al China to elucidate the mechanisms driving phyllosphere microbial diversity.

107 how anthropogenic disturbance may influence phyllosphere microbial dynamics and improves our underst

108 ge-scale and in-depth assessment of the rice phyllosphere microbiome aimed at identifying specific ho

109 discusses early efforts on GWAS of the plant phyllosphere microbiome and the outlook for future studi

110 itat for diverse microbes, and in return the phyllosphere microbiome greatly affects plant performanc

111 A workflow for GWAS of the phyllosphere microbiome is then presented, with particul

112 complex interactions between plants and the phyllosphere microbiome under global changes and to iden

113 ges in functional gene expression within the phyllosphere microbiome, resulting in enhanced gene abun

114 ted samples were characterized by a distinct phyllosphere microbiome, while the endosphere revealed a

115 s this question by selecting upon the tomato phyllosphere microbiome.

116 in Arabidopsis thaliana on the above-ground (phyllosphere) microbiome and determine the interacting i

117 The proficiency of phyllosphere microbiomes in efficiently utilizing plant-

118 have revealed a more complete repertoire of phyllosphere microbiota across plant taxa and how plants

119 Pseudomonadales abundance, dysbiosis of the phyllosphere microbiota and consequently higher suscepti

120 )-domain protein, harbour altered endophytic phyllosphere microbiota and display leaf-tissue damage a

121 Phyllosphere microbiota differed significantly between p

122 evel and nurture the diversity of endophytic phyllosphere microbiota for survival and health in a mic

123 ins in modulating the community structure of phyllosphere microbiota in M. truncatula and provide new

124 How the phyllosphere microbiota influences the growth of individ

125 that integrates the beneficial effect of the phyllosphere microbiota into the leaf development progra

126 llel greenhouse experiments, rhizosphere and phyllosphere microbiota of con- and heterospecific hosts

127 Phyllosphere microbiota play crucial roles in supporting

128 Whether and how plants control phyllosphere microbiota to ensure plant health is not we

129 Our results suggest that phyllosphere microbiota, like rhizosphere microbiota, ca

130 d the composition and community structure of phyllosphere microbiota, promoting greater richness and

131 rentially expressed in the presence of their phyllosphere microbiota, whereas polyploids exhibit some

132 diverse microbial communities, known as the phyllosphere microbiota.

133 ship between plant secondary metabolites and phyllosphere microbiota.

134 to and regulate the level and composition of phyllosphere microbiota.

135 of microbes that collectively constitute the phyllosphere microbiota.

136 opod community structure but also impact the phyllosphere microbiota.

137 leaves were used rather than the inoculated phyllosphere microorganisms only, confirming the degrada

138 death relative to the population dynamics of phyllosphere microorganisms.

139 hemistry and repeated application may affect phyllosphere mycobiome.

140 es and is the most common Pseudomonas in the phyllosphere of European Arabidopsis thaliana population

141 nterica populations naturally decline in the phyllosphere of plants, M. quadrilineatus infestation fa

142 al communities in the soil, rhizosphere, and phyllosphere of tomato and chili plants grown with and w

143 of the most abundant bacterial genera in the phyllosphere of wild Arabidopsis thaliana, but relative

144 ganisms colonizing the plant rhizosphere and phyllosphere play crucial roles in plant growth and heal

145 AB-induced UV mutability was also tracked in phyllosphere populations of B86-17 for up to 5 days foll

146 es for distinguishing these processes within phyllosphere populations.

147 tanding of microbial interactions within the phyllosphere, provide insights into the evolution of epi

148 The phyllosphere provides a dynamic environment for prophage

149 The phyllosphere represents one of the most abundant habitat

150 lobacteriaceae strain was also isolated from phyllosphere samples which contains genes encoding both

151 abundance of CH3Cl-degrading bacteria in the phyllosphere suggests that CH3Cl-degrading bacteria co-d

152 These results suggest that the phyllosphere supports diverse and potentially abundant C

153 Because of water limitations on phyllosphere surfaces, bacterial colonists, including pa

154 thin-host abundance of most leaf microbiome (phyllosphere) taxa colonizing a native forb is amplified

155 The phyllosphere, the aerial part of the plant, provides a u

156 The phyllosphere--the aerial surfaces of plants, including l

157 monas hortorum pv. gardneri (Xhg), alter the phyllosphere to the benefit of S. enterica.

158 Phyllosphere was an important habitat for protists, domi

159 The microbial composition of the phyllosphere was diverse and strongly resembled the comp

160 Bacterial communities in the phyllosphere were dominated by a core microbiome of taxa

161 against fungal diseases; particularly in the phyllosphere where this species is frequently found.

162 is an antagonistic member of the A. thaliana phyllosphere, which reduces infection of A. thaliana by

163 l limited, particularly when considering the phyllosphere, which represents one of the largest microb

164 ike microbiomes of the soil, rhizosphere and phyllosphere, wood associated communities are shaped by